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首页> 外文期刊>Archives of Oral Biology >Antibacterial activity and cytotoxicity of two novel cross-linking antibacterial monomers on oral pathogens.
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Antibacterial activity and cytotoxicity of two novel cross-linking antibacterial monomers on oral pathogens.

机译:两种新型交联抗菌单体对口腔病原体的抗菌活性和细胞毒性。

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OBJECTIVES: The antibacterial activity and cytotoxicity of two novel cross-linking antibacterial monomers, 2-methacryloxylethyl dodecyl methyl ammonium bromide (MAE-DB) and 2-methacryloxylethyl hexadecyl methyl ammonium bromide (MAE-HB) were tested in this study. DESIGN: The minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) of unpolymerized MAE-DB and MAE-HB against eight strains of oral bacteria were tested using a broth dilution test. Time-kill determinations were performed to examine the kinetics of unpolymerized MAE-DB and MAE-HB against Streptococcus mutans UA159 and Streptococcus sanguinis ATCC6715. Bacterial morphology was observed using a field emission scanning electron microscope (Fe-SEM). The cytotoxicity of unpolymerized two new monomers and Bis-GMA on the human gingival fibroblast cell line H2620 was assessed using a methyl thiazolyl tetrazolium assay. RESULTS: Unpolymerized MAE-DB and MAE-HB showed strong bactericidal activity against oral bacteria. The MBC value of MAE-DB ranged from 12.2 to 24.4mug/ml and the MBC value of MAE-HB ranged from 6.2 to 48.8mug/ml. Time-kill determinations indicated that unpolymerized MAE-DB and MAE-HB had rapid killing effects against S. mutans UA159 and S. sanguinis ATCC6715 at the concentration of 4x MBC. The Fe-SEM observation showed that MAE-DB and MAE-HB could disturb the integrity of bacteria and cause lysis of bacterial cells. The median lethal concentration values on human gingival fibroblast for both monomers were between 10 and 20mug/ml, and greater than that of Bis-GMA. CONCLUSIONS: Unpolymerized MAE-DB and MAE-HB monomers had strong bactericidal activity against eight strains of oral bacteria. Their cytotoxicities were less than that of Bis-GMA.
机译:目的:本研究测试了两种新型交联抗菌单体2-甲基丙烯酰氧基乙基十二烷基甲基溴化铵(MAE-DB)和2-甲基丙烯酰氧基乙基十六烷基甲基溴化铵(MAE-HB)的抗菌活性和细胞毒性。设计:使用肉汤稀释试验,测试了未聚合的MAE-DB和MAE-HB对八种口腔细菌的最小抑菌浓度(MIC)和最小杀菌浓度(MBC)。进行时间杀灭测定以检查未聚合的MAE-DB和MAE-HB对变形链球菌UA159和血链球菌ATCC6715的动力学。使用场发射扫描电子显微镜(Fe-SEM)观察细菌形态。使用甲基噻唑基四唑鎓测定法评估未聚合的两种新单体和Bis-GMA对人牙龈成纤维细胞H2620的细胞毒性。结果:未聚合的MAE-DB和MAE-HB对口腔细菌显示出很强的杀菌活性。 MAE-DB的MBC值范围为12.2至24.4mug / ml,MAE-HB的MBC值范围为6.2至48.8mug / ml。时间杀伤测定表明,未聚合的MAE-DB和MAE-HB在4x MBC浓度下对变形链球菌UA159和血红链球菌ATCC6715具有快速的杀灭作用。 Fe-SEM观察表明,MAE-DB和MAE-HB可能干扰细菌的完整性并引起细菌细胞的溶解。两种单体在人牙龈成纤维细胞上的致死浓度中值在10至20 ug / ml之间,并且比Bis-GMA高。结论:未聚合的MAE-DB和MAE-HB单体对八种口腔细菌具有强的杀菌活性。它们的细胞毒性小于Bis-GMA。

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